Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca1 |
G |
A |
4: 53,059,253 (GRCm39) |
|
probably benign |
Het |
Actl6a |
T |
C |
3: 32,776,759 (GRCm39) |
|
probably benign |
Het |
Aoc1l1 |
A |
T |
6: 48,952,767 (GRCm39) |
T231S |
probably benign |
Het |
Aox1 |
T |
C |
1: 58,385,371 (GRCm39) |
|
probably benign |
Het |
Arrdc3 |
A |
G |
13: 81,031,973 (GRCm39) |
T69A |
probably damaging |
Het |
Bbs2 |
T |
C |
8: 94,808,627 (GRCm39) |
K360R |
probably null |
Het |
Cdh8 |
A |
T |
8: 100,006,250 (GRCm39) |
N112K |
probably damaging |
Het |
Ces5a |
A |
T |
8: 94,228,809 (GRCm39) |
F474I |
probably damaging |
Het |
Dync1i1 |
G |
A |
6: 5,915,876 (GRCm39) |
D253N |
probably damaging |
Het |
Fam227b |
A |
G |
2: 125,845,759 (GRCm39) |
L410P |
probably damaging |
Het |
Ihh |
A |
T |
1: 74,990,372 (GRCm39) |
M1K |
probably null |
Het |
Itga6 |
A |
G |
2: 71,669,060 (GRCm39) |
T617A |
probably benign |
Het |
Itpr1 |
T |
A |
6: 108,363,609 (GRCm39) |
C744S |
probably benign |
Het |
Kif5a |
T |
C |
10: 127,081,311 (GRCm39) |
I208V |
probably benign |
Het |
Lama4 |
A |
G |
10: 38,937,387 (GRCm39) |
K659R |
probably benign |
Het |
Lpin3 |
T |
A |
2: 160,734,310 (GRCm39) |
|
probably null |
Het |
Macf1 |
T |
A |
4: 123,270,309 (GRCm39) |
E6612V |
probably damaging |
Het |
Naip2 |
T |
C |
13: 100,298,362 (GRCm39) |
E558G |
probably benign |
Het |
Ncdn |
T |
C |
4: 126,643,833 (GRCm39) |
K330E |
probably benign |
Het |
Neb |
C |
T |
2: 52,073,287 (GRCm39) |
D1975N |
possibly damaging |
Het |
Nell1 |
T |
A |
7: 50,503,621 (GRCm39) |
N675K |
possibly damaging |
Het |
Nlrp6 |
GAGAAGAAGAAGAAGAAGAAGA |
GAGAAGAAGAAGAAGAAGA |
7: 140,504,026 (GRCm39) |
|
probably benign |
Het |
Or4f47 |
G |
A |
2: 111,972,968 (GRCm39) |
R226H |
probably benign |
Het |
Rnf43 |
A |
G |
11: 87,625,003 (GRCm39) |
E737G |
possibly damaging |
Het |
Sardh |
C |
A |
2: 27,129,473 (GRCm39) |
W275L |
probably damaging |
Het |
Sel1l2 |
C |
T |
2: 140,071,979 (GRCm39) |
|
probably benign |
Het |
Sipa1l2 |
G |
A |
8: 126,176,712 (GRCm39) |
H1185Y |
probably damaging |
Het |
Skp2 |
G |
A |
15: 9,117,012 (GRCm39) |
Q298* |
probably null |
Het |
Spag16 |
G |
A |
1: 69,934,439 (GRCm39) |
|
probably benign |
Het |
Spink14 |
A |
G |
18: 44,161,896 (GRCm39) |
|
probably benign |
Het |
Stk4 |
C |
T |
2: 163,942,448 (GRCm39) |
T360M |
probably benign |
Het |
Stx12 |
T |
A |
4: 132,598,960 (GRCm39) |
I43L |
probably benign |
Het |
Tmc1 |
T |
A |
19: 20,793,548 (GRCm39) |
I538F |
possibly damaging |
Het |
Tollip |
T |
C |
7: 141,438,292 (GRCm39) |
M209V |
probably benign |
Het |
Ttn |
A |
T |
2: 76,643,312 (GRCm39) |
S13202R |
probably damaging |
Het |
Vmn2r60 |
T |
A |
7: 41,786,211 (GRCm39) |
V338D |
probably damaging |
Het |
Vwa8 |
T |
C |
14: 79,263,471 (GRCm39) |
L767P |
probably damaging |
Het |
Zfp202 |
C |
T |
9: 40,122,792 (GRCm39) |
T518I |
probably damaging |
Het |
|
Other mutations in Fam151b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00799:Fam151b
|
APN |
13 |
92,614,361 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02253:Fam151b
|
APN |
13 |
92,614,435 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03084:Fam151b
|
APN |
13 |
92,604,534 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03130:Fam151b
|
APN |
13 |
92,586,701 (GRCm39) |
missense |
probably benign |
0.01 |
P0015:Fam151b
|
UTSW |
13 |
92,604,452 (GRCm39) |
critical splice donor site |
probably null |
|
R0067:Fam151b
|
UTSW |
13 |
92,610,504 (GRCm39) |
missense |
probably benign |
0.08 |
R0067:Fam151b
|
UTSW |
13 |
92,610,504 (GRCm39) |
missense |
probably benign |
0.08 |
R0348:Fam151b
|
UTSW |
13 |
92,586,689 (GRCm39) |
missense |
probably benign |
0.00 |
R1404:Fam151b
|
UTSW |
13 |
92,610,480 (GRCm39) |
missense |
probably damaging |
1.00 |
R1482:Fam151b
|
UTSW |
13 |
92,586,674 (GRCm39) |
missense |
probably benign |
0.03 |
R1837:Fam151b
|
UTSW |
13 |
92,610,639 (GRCm39) |
intron |
probably benign |
|
R1891:Fam151b
|
UTSW |
13 |
92,586,678 (GRCm39) |
missense |
probably benign |
0.00 |
R1957:Fam151b
|
UTSW |
13 |
92,614,411 (GRCm39) |
missense |
probably damaging |
1.00 |
R1957:Fam151b
|
UTSW |
13 |
92,614,410 (GRCm39) |
missense |
probably damaging |
1.00 |
R2175:Fam151b
|
UTSW |
13 |
92,614,426 (GRCm39) |
missense |
probably damaging |
0.99 |
R4583:Fam151b
|
UTSW |
13 |
92,604,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R6762:Fam151b
|
UTSW |
13 |
92,604,558 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8153:Fam151b
|
UTSW |
13 |
92,614,410 (GRCm39) |
missense |
probably damaging |
1.00 |
R8881:Fam151b
|
UTSW |
13 |
92,604,630 (GRCm39) |
missense |
probably benign |
0.00 |
R8950:Fam151b
|
UTSW |
13 |
92,610,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R9497:Fam151b
|
UTSW |
13 |
92,610,621 (GRCm39) |
missense |
probably damaging |
0.99 |
X0021:Fam151b
|
UTSW |
13 |
92,586,734 (GRCm39) |
missense |
probably benign |
0.06 |
|